Reynolds R, Cenci di Bello I, Dawson M, Levine J
Department of Neuroinflammation, Division of Neuroscience, Imperial College School of Medicine, Charing Cross Campus, Fulham Palace Road, London W6 8RF, UK.
Prog Brain Res. 2001;132:165-74. doi: 10.1016/s0079-6123(01)32073-3.
Cells with the phenotypic characteristics of oligodendrocyte progenitors (NG2+/PDGF alpha R+/O4+) are found throughout the adult mammalian CNS in numbers similar to microglia. They are a reactive glial cell population and respond to demyelination by increasing in number, thereby repopulating the lesion site with cells capable of differentiating into remyelinating oligodendrocytes. Direct evidence that they differentiate into remyelinating cells is missing, although this is the most likely scenario. Cells with the same phenotype are found in normal human CNS tissue and also in chronic MS lesions. Further studies on this intriguing cell type are necessary in order to understand the molecular signals involved in their reaction to injury, particularly in multiple sclerosis.
具有少突胶质前体细胞表型特征(NG2+/血小板衍生生长因子α受体+/O4+)的细胞在成年哺乳动物的整个中枢神经系统中均有发现,其数量与小胶质细胞相似。它们是一种反应性胶质细胞群体,在脱髓鞘时数量会增加,从而使损伤部位重新填充能够分化为再髓鞘化少突胶质细胞的细胞。尽管这是最有可能的情况,但目前仍缺乏它们分化为再髓鞘化细胞的直接证据。在正常人类中枢神经系统组织以及慢性多发性硬化症病灶中也发现了具有相同表型的细胞。为了了解它们对损伤反应所涉及的分子信号,尤其是在多发性硬化症中的情况,有必要对这种有趣的细胞类型进行进一步研究。